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Mario Mastrangelo

Showing results (41-50 of 84) with videos related to

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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 7, 2009
New trends in neuronal migration disordersAlberto Verrotti, Alberto Spalice, Fabiana Ursitti, et al.
Frontiers in Neurology|December 20, 2023
Case report: Childhood epilepsy and borderline intellectual functioning hiding an AADC deficiency disorder associated with compound heterozygous <i>DDC</i> gene pathogenic variantsIda Cursio, Sabrina Siliquini, Claudia Carducci, et al.
Journal of Pediatric Genetics|February 21, 2022
Neurodevelopmental Impairment As the Main Phenotypic Hallmark Associated with the Translocation t(7;10)(7p22.3;q26.11)Mario Mastrangelo, Barbara Torres, Gloria De Vita, et al.
Neuropediatrics|July 2, 2025
Developmental and Epileptic Encephalopathy as a Novel Clinical Hallmark of SCA21Mario Mastrangelo, Giacomina Ricciardi, Carlo Greco, et al.
Minerva Pediatrics|May 31, 2023
Clinical profiles of acute arterial ischemic neonatal strokeMario Mastrangelo, Rossella Bove, Giacomina Ricciardi, et al.
Children (Basel, Switzerland)|June 24, 2022
Loss of Continuity of Care in Pediatric Neurology Services during COVID-19 Lockdown: An Additional Stressor for ParentsSerena Cesario, Consuelo Basile, Matteo Trevisan, et al.
Molecular Genetics and Metabolism Reports|August 31, 2019
Broadening phenotype of adenylosuccinate lyase deficiency: A novel clinical pattern resembling neuronal ceroid lipofuscinosisMario Mastrangelo, Chiara Alfonsi, Isabella Screpanti, et al.
Parkinsonism & Related Disorders|September 12, 2022
Long-term neurological and psychiatric outcomes in patients with aromatic l-amino acid decarboxylase deficiencyFilippo Manti, Mario Mastrangelo, Roberta Battini, et al.
Genes|February 25, 2023
Phenotypes and Genotypes of Inherited Disorders of Biogenic Amine Neurotransmitter MetabolismMario Mastrangelo, Manuela Tolve, Cristiana Artiola, et al.
European Journal of Pediatrics|July 2, 2024
The diagnostic and prognostic role of cerebrospinal fluid biomarkers in glucose transporter 1 deficiency: a systematic reviewMario Mastrangelo, Filippo Manti, Giacomina Ricciardi, et al.
Pageof 9

Showing results (41-50 of 84) with videos related to

Sort By:
Pageof 9
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 7, 2009
New trends in neuronal migration disordersAlberto Verrotti, Alberto Spalice, Fabiana Ursitti, et al.
Frontiers in Neurology|December 20, 2023
Case report: Childhood epilepsy and borderline intellectual functioning hiding an AADC deficiency disorder associated with compound heterozygous <i>DDC</i> gene pathogenic variantsIda Cursio, Sabrina Siliquini, Claudia Carducci, et al.
Journal of Pediatric Genetics|February 21, 2022
Neurodevelopmental Impairment As the Main Phenotypic Hallmark Associated with the Translocation t(7;10)(7p22.3;q26.11)Mario Mastrangelo, Barbara Torres, Gloria De Vita, et al.
Neuropediatrics|July 2, 2025
Developmental and Epileptic Encephalopathy as a Novel Clinical Hallmark of SCA21Mario Mastrangelo, Giacomina Ricciardi, Carlo Greco, et al.
Minerva Pediatrics|May 31, 2023
Clinical profiles of acute arterial ischemic neonatal strokeMario Mastrangelo, Rossella Bove, Giacomina Ricciardi, et al.
Children (Basel, Switzerland)|June 24, 2022
Loss of Continuity of Care in Pediatric Neurology Services during COVID-19 Lockdown: An Additional Stressor for ParentsSerena Cesario, Consuelo Basile, Matteo Trevisan, et al.
Molecular Genetics and Metabolism Reports|August 31, 2019
Broadening phenotype of adenylosuccinate lyase deficiency: A novel clinical pattern resembling neuronal ceroid lipofuscinosisMario Mastrangelo, Chiara Alfonsi, Isabella Screpanti, et al.
Parkinsonism & Related Disorders|September 12, 2022
Long-term neurological and psychiatric outcomes in patients with aromatic l-amino acid decarboxylase deficiencyFilippo Manti, Mario Mastrangelo, Roberta Battini, et al.
Genes|February 25, 2023
Phenotypes and Genotypes of Inherited Disorders of Biogenic Amine Neurotransmitter MetabolismMario Mastrangelo, Manuela Tolve, Cristiana Artiola, et al.
European Journal of Pediatrics|July 2, 2024
The diagnostic and prognostic role of cerebrospinal fluid biomarkers in glucose transporter 1 deficiency: a systematic reviewMario Mastrangelo, Filippo Manti, Giacomina Ricciardi, et al.
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